ARVD1: Difference between revisions
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(Created page with "__NOTOC__ {{Arrhythmogenic right ventricular dysplasia}} {{CMG}} {{SK}} Arrhythmogenic right ventricular dysplasia type 1; ==Overview== ==Pathophysiology== ===Genetics=== =...") |
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==Pathophysiology== | ==Pathophysiology== | ||
===Genetics=== | ===Genetics=== | ||
There is an [[autosomal dominant]] pattern of inheritance. This variant is due to a heterozygous mutation in the [[TGFB3]] gene ([http://omim.org/entry/190230 190230]) on chromosome 14q24. | |||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== |
Revision as of 23:36, 22 September 2012
Arrhythmogenic right ventricular dysplasia Microchapters |
Differentiating Arrhythmogenic right ventricular dysplasia from other Diseases |
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Diagnosis |
Treatment |
ARVD1 On the Web |
American Roentgen Ray Society Images of ARVD1 |
Directions to Hospitals Treating Arrhythmogenic right ventricular dysplasia |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 1;
Overview
Pathophysiology
Genetics
There is an autosomal dominant pattern of inheritance. This variant is due to a heterozygous mutation in the TGFB3 gene (190230) on chromosome 14q24.